Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_assertion description "[Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_assertion evidence source_evidence_literature NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_assertion SIO_000772 20094846 NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_assertion wasDerivedFrom befree-20140225 NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_assertion wasGeneratedBy ECO_0000203 NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP773574.RArlc_qnrRQpeV99E9uATE4FiCALhgRUC6XAXxAm5uWaM130_provenance.